SNOMED Clinical Terms - Infantile myofibromatosis | NCBO BioPortal

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Preferred Name	Infantile myofibromatosis
Synonyms	Congenital generalised fibromatosis Congenital generalized fibromatosis Infantile myofibromatosis (disorder)
ID	254146000
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/254146000
CONCEPTSTATUS	0
CTV3ID	X78Bv
has_associated_morphology	Myofibromatosis
has_finding_site	Structure of musculoskeletal system
inverse_may_be_a	Myofibromatosis Myofibromatosis
isa	Musculoskeletal fibromatosis Congenital disease Deep fibromatosis Neoplasm of musculoskeletal system
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Disease or Syndrome
SNOMEDID	D1-61630
SYNONYM FN	Infantile myofibromatosis (disorder)
SYNONYM SY	Congenital generalized fibromatosis
SYNONYM SYGB	Congenital generalised fibromatosis
TUI	T047
UMLS_CUI	C0432284

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://www.orphanet.org/rdfns#pat_id_3545	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://bioontology.org/projects/ontologies/radlex/radlexOwlDlComponent#RID4299	RadLex	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_3545	Experimental Factor Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X78Bv	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0432284	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X78Bv	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/228550	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0432284	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X77oZ	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0432284	skos:closeMatch	loom	04/02/13	View Notes

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